Microgliosis: a double‐edged sword in the control of food intake

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Salvi, Juliette | Andreoletti, Pierre | Audinat, Etienne | Balland, Eglantine | Ben Fradj, Selma | Cherkaoui-Malki, Mustapha | Heurtaux, Tony | Liénard, Fabienne | Nédélec, Emmanuelle | Rovère, Carole | Savary, Stéphane | Véjux, Anne | Trompier, Doriane | Benani, Alexandre

Edité par CCSD ; Wiley -

State-of-the-Art review.. International audience. Maintaining energy balance is essential for survival and health. This physiological function is controlled by the brain, which adapts food intake to energy needs. Indeed, the brain constantly receives a multitude of biological signals that are derived from digested foods, or that originate from the gastrointestinal tract, energy stores (liver and adipose tissues), and from other metabolically active organs (muscles). These signals, which include circulating nutrients, hormones, and neuronal inputs from the periphery, collectively provide information on the overall energy status of the body. In the brain, several neuronal populations can specifically detect these signals. Nutrient-sensing neurons are found in discrete brain areas and are highly enriched in the hypothalamus. In turn, specialized brain circuits coordinate homeostatic responses acting mainly on appetite, peripheral metabolism, activity and arousal. Accumulating evidence shows that hypothalamic microglial cells located at the vicinity of these circuits can influence the brain control of energy balance. However, microglial cells could have opposite effects on energy balance, i.e., homeostatic or detrimental, and the conditions for this shift are not totally understood yet. One hypothesis relies on the extent of microglial activation, and nutritional lipids can considerably change it.

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